Understanding phosphate metabolism in cancer and metastasis
Project Number1DP2CA186753-01
Former Number1DP2OD017293-01
Contact PI/Project LeaderFIEDLER, DOROTHEA
Awardee OrganizationPRINCETON UNIVERSITY
Description
Abstract Text
DESCRIPTION (provided by applicant): Metabolic rewiring of tumor cells is generally regarded as a cancer hallmark, and it is widely appreciated that altered glucose and glutamine metabolism drives cancer cell proliferation. We hypothesize that a similar situation exists for the
phosphorus needs of tumor cells: Rapidly dividing cells should rely on a constant supply of phosphate and exhibit altered phosphate metabolism. Furthermore, we posit that the high local concentration of inorganic phosphate contributes to the highly prolific microenvironment in osteolytic bone metastasis and promotes metastasis progression. To date, very little is known about intracellular phosphate metabolism, and it has not been possible to correlate intracellular phosphate levels, and subsequent changes in phosphate metabolism, with increased tumor cell proliferation. To elucidate whether a scenario of "phosphate addiction" exists, the development of new tools is sorely needed, and is the goal of the current proposal. Using an interdisciplinary approach that combines synthetic chemistry with cell biology and metabolomics, our lab is addressing this hypothesis in the context of bone metastasis. We are developing small-molecule fluorescent phosphate sensors to measure phosphate release during osteolysis and phosphate uptake in adjacent metastatic breast cancer cells. In addition, we are determining how the metabolic network of these cells handles the phosphate surplus in the bone microenvironment. Applying newly developed capture reagents from our lab to enrich for the phospho-metabolome, in combination with global metabolomics, will provide a wealth of information on phosphate-dependent metabolic rewiring. Overall, we hope to change the way phosphate is viewed: Instead of considering phosphate as a passive building block, it should be recognized as an active regulator of cellular metabolism and behavior. Understanding the metabolic requirements for successful colonization can lead to the development of effective therapies for patients with already-established metastases. These therapies are critically needed, as tumors are generally considered incurable once they have metastasized to bone.
Public Health Relevance Statement
Public Health Relevance Statement
Once tumors have metastasized to bone, they are generally considered incurable. The proposed research
seeks to understand the metabolic underpinnings that lead to successful bone colonization and metastasis
progression. This knowledge can then be exploited for the design and development of therapeutic strategies
against bone metastases, thereby improving the prognosis for hundreds of thousands of patients in the
United States.
NIH Spending Category
Cancer
Project Terms
AddressBehaviorBiochemical PathwayBreast Cancer CellCell ProliferationCellsCellular biologyDevelopmentExhibitsGlucoseGlutamineGoalsLeadMalignant NeoplasmsMeasuresMetabolicMetabolismMetastatic Neoplasm to the BoneNeoplasm MetastasisOsteolysisOsteolyticPatientsPhosphorusReagentSynthesis Chemistryaddictionbonecancer celleffective therapyinorganic phosphateinterdisciplinary approachmetabolomicsneoplastic cellsensorsmall moleculetooltumoruptake
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